Drug recall
Red Blood Cells Leukocytes Reduced
FDA recall event 47612 · Class II · LifeServe Blood Center
Key facts
| Event ID | 47612 |
|---|---|
| Recall numbers | B-0898-13 |
| Recalling firm | LifeServe Blood Center |
| Product type | Biologics |
| Products | Red Blood Cells Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor possibly at increased risk for Creutzfeldt-Jakob Disease (CJD), was distributed. |
| Initiation date | Feb 25, 2008 |
| Report date | Feb 20, 2013 |
| Termination date | Feb 12, 2013 |
| City | Des Moines |
| State | IA |
| Country | United States |
| FEI number | 1970355 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: